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Press Release : FDA accepts the new drug application for review of Idorsia's daridorexant for the treatment of adult patients with insomnia


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The application includes robust data from the Phase 3
registration program, which demonstrated efficacy of daridorexant on
objective and subjective sleep parameters, and an improvement in daytime
functioning, while maintaining a favorable safety profile
Allschwil, Switzerland March 10, 2021
Idorsia Ltd (SIX: IDIA) today announced that the US Food and Drug
Administration (FDA) has accepted the new drug application (NDA) for
review of Idorsia s investigational dual orexin receptor antagonist,
daridorexant, for the treatment of adult patients with insomnia.
Insomnia is a common problem with approximately 25 million adults in the
US who meet the diagnostic criteria. Insomnia, a condition of overactive ....

Switzerland General , Jean Paul Clozel , Idorsia Ltd , European Union , Drug Administration , Paul Clozel , Chief Executive Officer , Insomnia Daytime Symptoms , Dow Jones , Idorsia Ltd Stock Exchange , Press Release , An Idia Ch0363463438 , சுவிட்சர்லாந்து ஜநரல் , ஐரோப்பிய தொழிற்சங்கம் , தலைமை நிர்வாகி அதிகாரி , தூக்கமின்மை பகல்நேரம் அறிகுறிகள் , டோ ஜோன்ஸ் , ப்ரெஸ் வெளியீடு ,